Canonical Allele Identifier: CA5422729

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16869750C>T , CM000672.2:g.16869750C>T	GRCh38
NC_000010.10:g.16911749C>T , CM000672.1:g.16911749C>T	GRCh37
NC_000010.9:g.16951755C>T	NCBI36
NG_008967.1:g.265068G>A , LRG_540:g.265068G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.9340G>A MANE Select	ENSP00000367064.4:p.Gly3114Ser
ENST00000377833.8:c.9340G>A	ENSP00000367064.4:p.Gly3114Ser
NM_001081.3:c.9340G>A , LRG_540t1:c.9340G>A	NP_001072.2:p.Gly3114Ser
XM_011519709.1:c.5326G>A	XP_011518011.1:p.Gly1776Ser
XM_011519710.1:c.5302G>A	XP_011518012.1:p.Gly1768Ser
XM_011519711.1:c.5182G>A	XP_011518013.1:p.Gly1728Ser
XM_011519709.2:c.5326G>A	XP_011518011.1:p.Gly1776Ser
XM_011519710.2:c.5302G>A	XP_011518012.1:p.Gly1768Ser
XM_011519711.3:c.5182G>A	XP_011518013.1:p.Gly1728Ser
NM_001081.4:c.9340G>A MANE Select	NP_001072.2:p.Gly3114Ser